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Synthesis, Isolation and Crystal Structure Characterization of (Z)-4'-(1-Phenyl-2-p-tolylvinyl)biphenyl-4-carbaldehyde

  • Kim, Chul-Bae (School of Chemical Engineering and Materials Science, Chung-Ang University) ;
  • Jo, Hyun-jong (School of Chemical Engineering and Materials Science, Chung-Ang University) ;
  • Lee, Sung-Kyung (School of Chemical Engineering and Materials Science, Chung-Ang University) ;
  • Park, Kwang-Yong (School of Chemical Engineering and Materials Science, Chung-Ang University)
  • Published : 2009.10.20
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References

  1. Nolan, E. M.; Lippard, S. L. Acc. Chem. Res. 2009, 42, 193. https://doi.org/10.1021/ar8001409
  2. Gonçalves, M. S. T. Chem. Rev. 2009, 109, 190. https://doi.org/10.1021/cr0783840
  3. Jose, J.; Burgess, K. Tetrahedron 2006, 62, 11021. https://doi.org/10.1016/j.tet.2006.08.056
  4. Wang, F.; Tan, W. B.; Zhang, Y.; Fan, X.; Wang, M. Nanotechnol. 2006, 17, R1. https://doi.org/10.1088/0957-4484/17/1/R01
  5. Oliveira, O. N., Jr.; Dos Santos, D. S., Jr.; Balogh, D. T.; Zucolotto, V.; Mendonca, C. R. Adv. Colloid Interface Sci. 2005, 116, 179. https://doi.org/10.1016/j.cis.2005.05.008
  6. Cappitelli, F.; Sorlini, C. Crit. Rev. Microbiol. 2005, 31, 1. https://doi.org/10.1080/10408410490884766
  7. Li, G.; Shrotriya, V.; Yao, Y.; Huang, J.; Yang, Y. J. Mater. Chem. 2007, 17, 3126. https://doi.org/10.1039/b703075b
  8. Günes, S.; Neugebauer, H.; Sariciftci, N. S. Chem. Rev. 2007, 107, 1324. https://doi.org/10.1021/cr050149z
  9. Benanti, T. L.; Venkataraman, D. Photosynth. Res. 2006, 87, 73. https://doi.org/10.1007/s11120-005-6397-9
  10. Coakley, K. M.; McGehee, M. D. Chem. Mater. 2004, 16, 4533. https://doi.org/10.1021/cm049654n
  11. Kalinowski, J. Opt. Mater. 2008, 30, 792. https://doi.org/10.1016/j.optmat.2007.02.041
  12. Geffroy, B.; le Roy, P.; Prat, C. Polym. Int. 2006, 55, 572. https://doi.org/10.1002/pi.1974
  13. Veinot, J. G. C.; Marks, T. J. Acc. Chem. Res. 2005, 38, 632. https://doi.org/10.1021/ar030210r
  14. Shih, P.-I.; Shu, C.-F.; Tung, Y.-L.; Chi, Y. Appl. Phys. Lett. 2006, 88, 251110. https://doi.org/10.1063/1.2214141
  15. Raghunath, P.; Reddy, M. A.; Gouri, C.; Bhanuparakash, K.; Rao, V. J. J. Phys. Chem. A 2006, 110, 1152. https://doi.org/10.1021/jp0555753
  16. Wen, S.-W.; Lee, M.-T.; Chen, H. C. J. Display Technol. 2005, 1, 90. https://doi.org/10.1109/JDT.2005.852802
  17. Cocherel, N.; Poriel, C.; Rault-Berthelot, J.; Barrière, F.; Audebrand, N.; Slawin, A. M. Z.; Vignau, L. Chem. Eur. J. 2008, 14, 11328. https://doi.org/10.1002/chem.200801428
  18. Spehr, T.; Siebert, A.; Fuhrmann-Lieker, T.; Salbeck, J.; Rabe, T.; Riedl, T.; Johannes, H. H.; Kowalsky, W.; Wang, J.; Weimann, T.; Hinze, P. Appl. Phys. Lett. 2005, 87, 161103. https://doi.org/10.1063/1.2105996
  19. Schneider, D.; Rabe, T.; Riedl, T.; Dobbertin, T.; Kröger, M.; Becker, E.; Johannes, H. H.; Kowalsky, W.; Weimann, T.; Wang, J.; Hinze, P. J. Appl. Phys. 2005, 98, 043104. https://doi.org/10.1063/1.1991967
  20. Johansson, N.; Salbeck, J.; Bauer, J.; Weiss$\ddot{o}$rtel, F.; Bröms, P.; Andersson, A.; Salaneck, W. R. Adv. Mater. 1998, 10, 1136.
  21. Jarikov, V. V. Appl. Phys. Lett. 2008, 92, 244103. https://doi.org/10.1063/1.2939099
  22. Zehm, D.; Fudikar, W.; Hans, M.; Schilde, U.; Kelling, A.; Linker, T. Chem. Eur. J. 2008, 14, 11429. https://doi.org/10.1002/chem.200801355
  23. Martin, R.; Teruel, L.; Aprile, C.; Cabeza, J. F.; Alvaro, M.; Garcia, H. Tetrahedron 2008, 64, 6270. https://doi.org/10.1016/j.tet.2008.04.112
  24. Martin, R.; Benítez, M.; Cabeza, J. F.; García, H.; Leyva, A. J. Phys. Chem. C 2007, 111, 7532. https://doi.org/10.1021/jp0687394
  25. Grimsdale, A. C.; Chan, K. L.; Martin, R. E.; Jokisz, P. G.; Holmes, A. Chem. Rev. 2009, 109, 897. https://doi.org/10.1021/cr000013v
  26. Praveen, V. K.; Babu, S. S.; Vijayakumar, C.; Varghese, R.; Ajayaghosh, A. Bull. Chem. Soc. Jpn. 2008, 81, 1196. https://doi.org/10.1246/bcsj.81.1196
  27. Babudri, F.; Farinola, G. M.; Naso, F. J. Mater. Chem. 2004, 14, 11. https://doi.org/10.1039/b309515k
  28. Yamamoto, T. Macromol. Rapid Commun. 2002, 23, 583. https://doi.org/10.1002/1521-3927(20020701)23:10/11<583::AID-MARC583>3.0.CO;2-I
  29. Rausch, A. F.; Thompson, M. E.; Yersin, H. Inorg. Chem. 2009, 48, 1928. https://doi.org/10.1021/ic801250g
  30. Su, S.-J.; Takahashi, Y.; Chiba, T.; Takeda, T.; Kido, J. Adv. Funct. Mater. 2009, 19, 1260. https://doi.org/10.1002/adfm.200800809
  31. Xu, Y.; Yang, R.; Peng, J.; Mikhailovsky, A. A.; Cao, Y.; Nguyen, T.-Q.; Bazan, G. C. Adv. Mater. 2009, 21, 584. https://doi.org/10.1002/adma.200802548
  32. Chen, F.-C.; Chien, S.-C.; Chen, Y.-S. Appl. Phys. Lett. 2009, 94, 043306. https://doi.org/10.1063/1.3075066
  33. Hosokawa, C.; Higashi, H.; Nakamura, H.; Kusumoto, T. Appl. Phys. Lett. 1995, 67, 3853. https://doi.org/10.1063/1.115295
  34. Hosokawa, C.; Tokailin, H.; Higashi, H.; Kusumoto, T. J. Appl. Phys. 1995, 78, 5831. https://doi.org/10.1063/1.359650
  35. Hosokawa, C.; Higashi, H.; Kusumoto, T. Appl. Phys. Lett. 1993, 62, 3238. https://doi.org/10.1063/1.109085
  36. Williams, R. T.; Hodge, P.; Yeates, S. G. Polym. Adv. Technol. 2008, 19, 569. https://doi.org/10.1002/pat.1108
  37. Williams, R. T.; Hodge, P.; Yeates, S. G. React. Funct. Polym. 2007, 67, 1061. https://doi.org/10.1016/j.reactfunctpolym.2007.06.006
  38. Su, H.-J.; Wu, F.-I.; Tseng, Y.-H.; Shu, C.-F. Adv. Funct. Mater. 2005, 15, 1209. https://doi.org/10.1002/adfm.200400269
  39. Chen, Y.; Lai, S.-P. J. Polym. Sci. Part A: Polym. Chem. 2001, 39, 2571. https://doi.org/10.1002/pola.1234
  40. Fischer, A.; Chénais, S; Forget, S.; Castex, M.-C. ; Adès, D.; Siove, A.; Denis, C.; Maisse, P.; Geffroy, B. J. Phys. D: Appl. Phys. 2005, 39, 917. https://doi.org/10.1088/0022-3727/39/5/004
  41. Wu, F.-I.; Shih, P. I.; Yuan, M.-C.; Dixit, A. K.; Shu, C.-F.; Chung, Z.-M.; Diau, E. W.-G. J. Mater. Chem. 2005, 15, 4753. https://doi.org/10.1039/b510035f
  42. Liao, C.-H.; Lee, M.-T.; Tsai, C.-H.; Chen, C. H. Appl. Phys. Lett. 2005, 86, 203507. https://doi.org/10.1063/1.1931052
  43. Joswick, M. D.; Campbell, I. H.; Barashkov, N. N.; Ferraris, J. P. J. Appl. Phys. 1996, 80, 2883. https://doi.org/10.1063/1.363140
  44. Liu, S.; He, F.; Wang, H.; Xu, H.; Wang, C.; Li, F.; Ma, Y. J. Mater. Chem. 2008, 18, 4802. https://doi.org/10.1039/b807266c
  45. Wang, S.; Oldham, W. J.; Hudack, R. A.; Bazan, G. C. J. Am. Chem. Soc. 2000, 122, 5695. https://doi.org/10.1021/ja992924w
  46. Wadsworth, W. W.; Emmons, W. D. J. Am. Chem. Soc. 1961, 83, 1733. https://doi.org/10.1021/ja01468a042
  47. Rigamonti, L.; Babgi, B.; Cifuentes, M. P.; Roberts, R. L.; Petrie, S.; Stranger, R.; Righetto, S.; Teshome, A.; Asselberghs, I.; Clays, K.; Humphrey, M. G. Inorg. Chem. 2009, 48, 3562. https://doi.org/10.1021/ic801953z
  48. Snyder, S. A.; Breazzano, S. P.; Ross, A. G.; Lin, Y.; Zografos, A. L. 2009, 131, 1753. https://doi.org/10.1021/ja806183r
  49. Babu, S. S.; Praveen, V. K.; Prasanthkumar, S.; Ajayaghosh, A. Chem. Eur. J. 2008, 14, 9577. https://doi.org/10.1002/chem.200801255
  50. Kabir, M. S.; Engelbrecht, K.; Polanowski, R.; Krueger, S. M.; Ignasiak, R.; Rott, M.; Schwan, W. R.; Stemper, M. E.; Reed, K. D.; Sherman, D.; Cook, J. M. Bioorg. Med. Chem. Lett. 2008, 18, 5745. https://doi.org/10.1016/j.bmcl.2008.09.085
  51. Feng, X.; Feng, F.; Yu, M.; He, F.; Xu, Q.; Tang, H.; Wang, S.; Li, Y.; Zhu, D. Org. Lett. 2008, 10, 5369. https://doi.org/10.1021/ol802210s
  52. McGrier, P. L.; Solntsev, K. M.; Miao, S.; Tolbert, L. M.; Miranda, O. R.; Rotello, V. M.; Bunz, U. H. F. Chem. Eur. J. 2008, 14, 4503. https://doi.org/10.1002/chem.200800296
  53. Cho, C.-H.; Park, K. Bull. Korean Chem. Soc. 2007, 28, 1159 https://doi.org/10.5012/bkcs.2007.28.7.1159
  54. Kim, C.-B.; Cho, C.-H.; Chai, K. Y.; Park, K. Acta Cryst. E 2008, E64, o457.
  55. Büttner, M. W.; Burschka, C.; Daiss, J. O.; Ivanova, D.; Rochel, N.; Kammerer, S.; Peluso-Iltis, C.; Bindler, A.; Gaudon, C.; Germain, P.; Moras, D.; Gronemeyer, H.; Tacke, R. ChemBioChem 2007, 8, 1688. https://doi.org/10.1002/cbic.200700182
  56. Leonik, F. M.; Papke, R. L.; Horenstein, N. A. Bioorg. Med. Chem. Lett. 2007, 17, 1520. https://doi.org/10.1016/j.bmcl.2007.01.003
  57. Pandey, R. K.; Wakharkar, R. D.; Kumar, P. Synth. Commun. 2005, 35, 2795. https://doi.org/10.1080/00397910500290516
  58. Fernández-Gacio, A.; Vitale, C.; Mourino, A. J. Org. Chem. 2000, 65, 6978. https://doi.org/10.1021/jo000579j
  59. Ginocchietti, G.; Galiazzo, G.; Pannacci, D.; Mazzucato, U.; Spalletti, A. Chem. Phys. 2006, 331, 164. https://doi.org/10.1016/j.chemphys.2006.10.008
  60. Gao, L.; Peng, H.; He, H.-W. Acta Cryst. E 2006, E62, o5032.
  61. De Borger, R.; Vande Velde, C. M. L.; Blockhuys, F. Acta Cryst. E 2005, E61, o819.
  62. Ogawa, K.; Sabo, T.; Yoshimura, S.; Takeuchi, Y.; Toriumi, K. J. Am. Chem. Soc. 1992, 114, 1041. https://doi.org/10.1021/ja00029a037
  63. Barnes, J. C.; Chudek, J. A. Acta Cryst. E 2002, E58, o603.
  64. SethuSankar, K.; Saravanan, S.; Velmurugan, D.; Parvez, M. Acta Cryst. C 2003, C59, p156.
  65. SMART, Version 5.0, Data Collection Software, Bruker AXS Inc., Madison, WI, 1998.
  66. SAINT, Version 5.0, Data Integration Software, Bruker AXS Inc., Madison, WI, 1998.
  67. Sheldrick, G. M. SADABS, Program for Absorption Correction with Bruker SMART system, Universitat Gttingen, Germany, 1996.

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